Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_assertion description "[Molecular cloning and characterization of a full-length complementary DNA encoding human acid ceramidase. Identification Of the first molecular lesion causing Farber disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_assertion evidence source_evidence_literature NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_assertion SIO_000772 8955159 NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_assertion wasDerivedFrom befree-20140225 NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_assertion wasGeneratedBy ECO_0000203 NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP491659.RA961vTaTxnvVnL-hcCwGdv43kZ6vO9YYfibX-yfpjBrE130_provenance.